Canonical Allele Identifier: CA1468146831
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1719063535

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73418144_73418145del , CM000666.2:g.73418144_73418145del GRCh38
NC_000004.11:g.74283861_74283862del , CM000666.1:g.74283861_74283862del GRCh37
NC_000004.10:g.74502725_74502726del NCBI36
NG_009291.1:g.18890_18891del

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1485_1486del MANE Select ENSP00000295897.4:p.Asp495GlufsTer24
ENST00000295897.8:c.1485_1486del ENSP00000295897.4:p.Asp495GlufsTer24
ENST00000401494.7:c.1140_1141del ENSP00000384695.3:p.Asp380GlufsTer24
ENST00000415165.6:c.909_910del ENSP00000401820.2:p.Asp303GlufsTer24
ENST00000476441.6:c.*764_*765del ENSP00000423727.1:n.*764_*765del
ENST00000486939.1:n.139_140del
ENST00000503124.5:c.1035_1036del ENSP00000421027.1:p.Asp345GlufsTer24
ENST00000505649.5:n.1032_1033del
ENST00000509063.5:c.1485_1486del ENSP00000422784.1:p.Asp495GlufsTer24
ENST00000511370.1:c.1018_1019del
ENST00000621085.4:c.846_847del ENSP00000483421.1:p.Asp282GlufsTer24
ENST00000621628.4:c.846_847del ENSP00000480485.1:p.Asp282GlufsTer24
NM_000477.5:c.1485_1486del NP_000468.1:p.Asp495GlufsTer24
NM_000477.6:c.1485_1486del NP_000468.1:p.Asp495GlufsTer24
NM_000477.7:c.1485_1486del MANE Select NP_000468.1:p.Asp495GlufsTer24